Published in J Cell Biol on February 13, 2006
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies. J Biomed Biotechnol (2010) 2.01
Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation. Nat Rev Mol Cell Biol (2011) 1.91
Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I. Mol Cell Biol (2007) 1.82
Mba1, a membrane-associated ribosome receptor in mitochondria. EMBO J (2006) 1.50
Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly. EMBO J (2007) 1.47
Mechanism of protein biosynthesis in mammalian mitochondria. Biochim Biophys Acta (2011) 1.26
Cooperation of translocase complexes in mitochondrial protein import. J Cell Biol (2007) 1.26
Coa3 and Cox14 are essential for negative feedback regulation of COX1 translation in mitochondria. J Cell Biol (2010) 1.20
Mitochondrial protein synthesis, import, and assembly. Genetics (2012) 1.17
Roles of Oxa1-related inner-membrane translocases in assembly of respiratory chain complexes. Biochim Biophys Acta (2008) 1.13
Reconstitution of protein targeting to the inner envelope membrane of chloroplasts. J Cell Biol (2006) 1.13
Mitochondrial protein import and human health and disease. Biochim Biophys Acta (2006) 1.04
Role of mitochondrial inner membrane organizing system in protein biogenesis of the mitochondrial outer membrane. Mol Biol Cell (2012) 0.96
Perspectives on: SGP symposium on mitochondrial physiology and medicine: the pathophysiology of LETM1. J Gen Physiol (2012) 0.92
Novel components of an active mitochondrial K(+)/H(+) exchange. J Biol Chem (2010) 0.92
Oxa1-ribosome complexes coordinate the assembly of cytochrome C oxidase in mitochondria. J Biol Chem (2012) 0.89
Ribosome-binding proteins Mdm38 and Mba1 display overlapping functions for regulation of mitochondrial translation. Mol Biol Cell (2010) 0.89
Trypanosome Letm1 protein is essential for mitochondrial potassium homeostasis. J Biol Chem (2013) 0.88
MPV17L2 is required for ribosome assembly in mitochondria. Nucleic Acids Res (2014) 0.87
The mitochondrial oxidase assembly protein1 (Oxa1) insertase forms a membrane pore in lipid bilayers. J Biol Chem (2012) 0.86
LETM proteins play a role in the accumulation of mitochondrially encoded proteins in Arabidopsis thaliana and AtLETM2 displays parent of origin effects. J Biol Chem (2012) 0.86
Suppression of lung tumorigenesis by leucine zipper/EF hand-containing transmembrane-1. PLoS One (2010) 0.84
A complex of Cox4 and mitochondrial Hsp70 plays an important role in the assembly of the cytochrome c oxidase. Mol Biol Cell (2013) 0.81
A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations. BMC Med Genet (2015) 0.79
Protein biosynthesis in mitochondria. Biochemistry (Mosc) (2013) 0.76
LETM1 overexpression is correlated with the clinical features and survival outcome of breast cancer. Int J Clin Exp Pathol (2015) 0.75
The Degradation Pathway of the Mitophagy Receptor Atg32 Is Re-Routed by a Posttranslational Modification. PLoS One (2016) 0.75
Proteomic profiling of the mitochondrial ribosome identifies Atp25 as a composite mitochondrial precursor protein. Mol Biol Cell (2016) 0.75
Overlapping Role of Respiratory Supercomplex Factor Rcf2 and Its N-terminal Homolog Rcf3 in Saccharomyces cerevisiae. J Biol Chem (2016) 0.75
Mitochondrial respiratory-chain diseases. N Engl J Med (2003) 8.68
Protein import into mitochondria. Annu Rev Biochem (1997) 6.82
Characterization of the human heart mitochondrial proteome. Nat Biotechnol (2003) 5.66
The proteome of Saccharomyces cerevisiae mitochondria. Proc Natl Acad Sci U S A (2003) 5.13
Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae. Mol Biol Cell (2002) 3.27
New developments in mitochondrial assembly. Annu Rev Cell Dev Biol (2004) 3.07
Mitochondrial import and the twin-pore translocase. Nat Rev Mol Cell Biol (2004) 2.78
Mitochondrial presequence translocase: switching between TOM tethering and motor recruitment involves Tim21 and Tim17. Cell (2005) 2.49
Assaying protein import into mitochondria. Methods Cell Biol (2001) 2.04
The mitochondrial presequence translocase: an essential role of Tim50 in directing preproteins to the import channel. Cell (2002) 1.95
Membrane translocation of mitochondrially coded Cox2p: distinct requirements for export of N and C termini and dependence on the conserved protein Oxa1p. Mol Biol Cell (1997) 1.93
Oxa1p acts as a general membrane insertion machinery for proteins encoded by mitochondrial DNA. EMBO J (2001) 1.91
Protein insertion into the mitochondrial inner membrane by a twin-pore translocase. Science (2003) 1.89
Yeast Oxa1 interacts with mitochondrial ribosomes: the importance of the C-terminal region of Oxa1. EMBO J (2003) 1.83
Crystal structure of the yeast cytochrome bc1 complex with its bound substrate cytochrome c. Proc Natl Acad Sci U S A (2002) 1.82
Ribosome binding to the Oxa1 complex facilitates co-translational protein insertion in mitochondria. EMBO J (2003) 1.79
Oxa1p, an essential component of the N-tail protein export machinery in mitochondria. Proc Natl Acad Sci U S A (1998) 1.76
Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2. Am J Hum Genet (2003) 1.67
Intracellular calcium-binding proteins: more sites than insights. Trends Biochem Sci (1991) 1.66
Pam16 has an essential role in the mitochondrial protein import motor. Nat Struct Mol Biol (2004) 1.63
Oxa1p mediates the export of the N- and C-termini of pCoxII from the mitochondrial matrix to the intermembrane space. FEBS Lett (1997) 1.62
The LETM1/YOL027 gene family encodes a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome. J Biol Chem (2004) 1.49
Insertion of proteins into the inner membrane of mitochondria: the role of the Oxa1 complex. Biochim Biophys Acta (2002) 1.36
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation. Am J Med Genet (2001) 1.34
Protein import into and across the mitochondrial inner membrane: role of the TIM23 and TIM22 translocons. Biochim Biophys Acta (2002) 1.33
LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients. Genomics (1999) 1.32
The Alb3/Oxa1/YidC protein family: membrane-localized chaperones facilitating membrane protein insertion? Trends Cell Biol (2003) 1.31
Cloning of a human gene involved in cytochrome oxidase assembly by functional complementation of an oxa1- mutation in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A (1994) 1.22
The Oxa1 protein forms a homooligomeric complex and is an essential part of the mitochondrial export translocase in Neurospora crassa. J Biol Chem (2002) 1.21
Mba1, a novel component of the mitochondrial protein export machinery of the yeast Saccharomyces cerevisiae. J Cell Biol (2001) 1.17
Cox18p is required for export of the mitochondrially encoded Saccharomyces cerevisiae Cox2p C-tail and interacts with Pnt1p and Mss2p in the inner membrane. Mol Biol Cell (2002) 1.12
LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein. Genomics (2004) 1.11
Mutations affecting a yeast mitochondrial inner membrane protein, pnt1p, block export of a mitochondrially synthesized fusion protein from the matrix. Mol Cell Biol (1999) 1.10
The definition of mitochondrial H+ ATPase assembly defects in mit- mutants of Saccharomyces cerevisiae with a monoclonal antibody to the enzyme complex as an assembly probe. Biochim Biophys Acta (1988) 1.08
Absence of the mitochondrial AAA protease Yme1p restores F0-ATPase subunit accumulation in an oxa1 deletion mutant of Saccharomyces cerevisiae. J Biol Chem (2000) 1.08
Analysis of mitochondrial translation products in vivo and in organello in yeast. Methods Cell Biol (2001) 1.01
The Oxa2 protein of Neurospora crassa plays a critical role in the biogenesis of cytochrome oxidase and defines a ubiquitous subbranch of the Oxa1/YidC/Alb3 protein family. Mol Biol Cell (2004) 0.95
Mitochondrial disorders. Curr Opin Neurol (2003) 0.95
Peripheral mitochondrial inner membrane protein, Mss2p, required for export of the mitochondrially coded Cox2p C tail in Saccharomyces cerevisiae. Mol Cell Biol (2001) 0.93
Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206. Biochem J (2004) 0.92
A peptide preconcentration approach for nano-high-performance liquid chromatography to diminish memory effects. Proteomics (2004) 0.89
Mitochondrial disorders. Curr Neurol Neurosci Rep (2003) 0.89
Deletion of QCR6, the gene encoding subunit six of the mitochondrial cytochrome bc1 complex, blocks maturation of cytochrome c1, and causes temperature-sensitive petite growth in Saccharomyces cerevisiae. J Biol Chem (1994) 0.87
The proteome of Saccharomyces cerevisiae mitochondria. Proc Natl Acad Sci U S A (2003) 5.13
The impact of enhancing students' social and emotional learning: a meta-analysis of school-based universal interventions. Child Dev (2011) 4.81
A mitochondrial specific stress response in mammalian cells. EMBO J (2002) 3.95
Machinery for protein sorting and assembly in the mitochondrial outer membrane. Nature (2003) 3.46
Protein labeling by iTRAQ: a new tool for quantitative mass spectrometry in proteome research. Proteomics (2007) 2.97
Dissecting membrane insertion of mitochondrial beta-barrel proteins. Cell (2008) 2.97
Levels of human Fis1 at the mitochondrial outer membrane regulate mitochondrial morphology. J Cell Sci (2004) 2.78
Identification and functional characterization of microRNAs involved in the malignant progression of gliomas. Brain Pathol (2009) 2.67
An essential role of Sam50 in the protein sorting and assembly machinery of the mitochondrial outer membrane. J Biol Chem (2003) 2.59
Dual role of mitofilin in mitochondrial membrane organization and protein biogenesis. Dev Cell (2011) 2.52
Mitochondrial presequence translocase: switching between TOM tethering and motor recruitment involves Tim21 and Tim17. Cell (2005) 2.49
Crystal structure of the mitochondrial chaperone TIM9.10 reveals a six-bladed alpha-propeller. Mol Cell (2006) 2.46
Essential role of Mia40 in import and assembly of mitochondrial intermembrane space proteins. EMBO J (2004) 2.43
Cytoscape: software for visualization and analysis of biological networks. Methods Mol Biol (2011) 2.43
MiD49 and MiD51, new components of the mitochondrial fission machinery. EMBO Rep (2011) 2.26
Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients. J Mol Biol (2006) 2.21
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome. Am J Hum Genet (2010) 2.07
The mitochondrial morphology protein Mdm10 functions in assembly of the preprotein translocase of the outer membrane. Dev Cell (2004) 1.98
Mitochondrial preprotein translocase of trypanosomatids has a bacterial origin. Curr Biol (2011) 1.98
The mitochondrial presequence translocase: an essential role of Tim50 in directing preproteins to the import channel. Cell (2002) 1.95
Essential role of Isd11 in mitochondrial iron-sulfur cluster synthesis on Isu scaffold proteins. EMBO J (2005) 1.92
Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation. Nat Rev Mol Cell Biol (2011) 1.91
Protein insertion into the mitochondrial inner membrane by a twin-pore translocase. Science (2003) 1.89
Understanding mitochondrial complex I assembly in health and disease. Biochim Biophys Acta (2011) 1.86
Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I. Mol Cell Biol (2007) 1.82
Proteomic analysis of the yeast mitochondrial outer membrane reveals accumulation of a subclass of preproteins. Mol Biol Cell (2006) 1.75
A J-protein is an essential subunit of the presequence translocase-associated protein import motor of mitochondria. J Cell Biol (2003) 1.71
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. J Clin Invest (2004) 1.71
Assembly of mitochondrial complex I and defects in disease. Biochim Biophys Acta (2008) 1.67
Dissection of the mitochondrial import and assembly pathway for human Tom40. J Biol Chem (2005) 1.66
Motor-free mitochondrial presequence translocase drives membrane integration of preproteins. Nat Cell Biol (2007) 1.64
Mitochondrial protein-import machinery: correlating structure with function. Trends Cell Biol (2007) 1.64
Pam16 has an essential role in the mitochondrial protein import motor. Nat Struct Mol Biol (2004) 1.63
The regulation of mitochondrial morphology: intricate mechanisms and dynamic machinery. Cell Signal (2011) 1.62
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome. Curr Biol (2009) 1.62
Role of MINOS in mitochondrial membrane architecture: cristae morphology and outer membrane interactions differentially depend on mitofilin domains. J Mol Biol (2012) 1.61
Genome-wide characterization of miR-34a induced changes in protein and mRNA expression by a combined pulsed SILAC and microarray analysis. Mol Cell Proteomics (2011) 1.59
The morphology proteins Mdm12/Mmm1 function in the major beta-barrel assembly pathway of mitochondria. EMBO J (2007) 1.58
The amyloid precursor protein intracellular domain (AICD) as modulator of gene expression, apoptosis, and cytoskeletal dynamics-relevance for Alzheimer's disease. Prog Neurobiol (2008) 1.58
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease. Am J Hum Genet (2008) 1.58
Biogenesis of the protein import channel Tom40 of the mitochondrial outer membrane: intermembrane space components are involved in an early stage of the assembly pathway. J Biol Chem (2004) 1.55
Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome. Mol Biol Cell (2005) 1.55
Tim50 maintains the permeability barrier of the mitochondrial inner membrane. Science (2006) 1.55
Novel mitochondrial intermembrane space proteins as substrates of the MIA import pathway. J Mol Biol (2006) 1.53
Impaired folding of the mitochondrial small TIM chaperones induces clearance by the i-AAA protease. J Mol Biol (2012) 1.51
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. Ann Neurol (2004) 1.51
Mitochondrial morphology and distribution in mammalian cells. Biol Chem (2006) 1.49
Rcf1 mediates cytochrome oxidase assembly and respirasome formation, revealing heterogeneity of the enzyme complex. Cell Metab (2012) 1.48
Recent advances into the understanding of mitochondrial fission. Biochim Biophys Acta (2012) 1.48
Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly. EMBO J (2007) 1.47
Psb27, a cyanobacterial lipoprotein, is involved in the repair cycle of photosystem II. Plant Cell (2006) 1.46
Pex8p: an intraperoxisomal organizer of the peroxisomal import machinery. Mol Cell (2003) 1.45
Proteome-wide identification of mycobacterial pupylation targets. Mol Syst Biol (2010) 1.44
Import and assembly of proteins into mitochondria of mammalian cells. Biochim Biophys Acta (2002) 1.43
Regulation of mitochondrial protein import by cytosolic kinases. Cell (2011) 1.42
Proteomics characterization of mouse kidney peroxisomes by tandem mass spectrometry and protein correlation profiling. Mol Cell Proteomics (2007) 1.41
Impacts of stable element intake on 14C and 129I dose estimates. Health Phys (2005) 1.40
The essential mitochondrial protein Erv1 cooperates with Mia40 in biogenesis of intermembrane space proteins. J Mol Biol (2005) 1.40
Biochemical and molecular diagnosis of mitochondrial respiratory chain disorders. Biochim Biophys Acta (2004) 1.39
Oxygen tension regulates the expression of a group of procollagen hydroxylases. Eur J Biochem (2003) 1.38
Sam35 of the mitochondrial protein sorting and assembly machinery is a peripheral outer membrane protein essential for cell viability. J Biol Chem (2004) 1.37
Ubiquitination of the peroxisomal targeting signal type 1 receptor, Pex5p, suggests the presence of a quality control mechanism during peroxisomal matrix protein import. J Biol Chem (2004) 1.37
The cellular oxygen tension regulates expression of the endoplasmic oxidoreductase ERO1-Lalpha. Eur J Biochem (2003) 1.36
Sorting switch of mitochondrial presequence translocase involves coupling of motor module to respiratory chain. J Cell Biol (2007) 1.36
Pam17 is required for architecture and translocation activity of the mitochondrial protein import motor. Mol Cell Biol (2005) 1.34
Uniform nomenclature for the mitochondrial contact site and cristae organizing system. J Cell Biol (2014) 1.34
The presequence translocase-associated protein import motor of mitochondria. Pam16 functions in an antagonistic manner to Pam18. J Biol Chem (2004) 1.34